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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2258409Generated: October 31, 2026

Triethylamine → dibenzyl 4-[N,N-bis(2-chloroethyl)amino]phenylcarbamoyl-L-glutamate

https://huagongshe.com/reaction/2258409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriphosgeneHCID 94429—
ReactantL-Glutamic acid dibenzyl ester tosylateHCID 13233366—
Reactant4-[N,N-bis-(2-chloroethyl)amino]anilinium chlorideHCID 70222082—
SolventChloroformHCID 6212—
Productdibenzyl 4-[N,N-bis(2-chloroethyl)amino]phenylcarbamoyl-L-glutamateHCID 70224102—

Reaction Steps

To a solution of triphosgene (1 g) in chloroform (80 ml) was added at 10° C. 4-[N,N-bis-(2-chloroethyl)amino]anilinium chloride (2.7 g). Whilst keeping the tempeature at 10° C., triethylamine (4.15 ml) was added and the mixture was stirred and allowed to warm to ambient temperature for 15 minutes. To this mixture was added in one portion dibenzyl glutamate tosylate and triethylamine (1.7 ml). After 1.5 hours at ambient tempeature the mixture was diluted with chloroform (100 ml), washed twice with water, dried and evaporated to dryness. The resdiue was chromatographed on Merck silica gell Art 9385, eluting with ethyl acetate hexane to give dibenzyl 4[N,N-bis(2-chloroethyl)amino]-phenylcarbamoyl-L-glutamate (2.5 g). m.p. 119°-22° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05660829
Source datasetuspto-grants-1997_08
ORD IDord-2b03205782fd449f979d09c1771a542f
Source noteuspto-grants-1997_08